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Structure of 90600-20-7
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(S)-2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid is a chiral building block featuring a conjugated enoic acid moiety and a protected amine. This bench-stable, moisture-tolerant reagent integrates readily into peptide synthesis and heterocyclic scaffolds, enabling efficient access to bioactive analogs through orthogonal functionalization.
(S)-2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid serves as a versatile chiral building block for the synthesis of peptidomimetics and bioactive heterocycles. The pendant alkene enables efficient downstream functionalization via cross-coupling or hydrogenation, while the Boc-protected amine offers orthogonal stability and facile deprotection. Its bench-stable nature and compatibility with standard peptide coupling protocols facilitate streamlined access to complex scaffolds in medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: